ENST00000496887.7:c.236T>A
|
ENSP00000434560.2:p.Phe79Tyr
|
|
ENST00000646564.2:c.478-12788T>A
|
ENSP00000495806.2:n.478-12788T>A
|
|
ENST00000155840.12:c.497T>A
MANE Select
|
ENSP00000155840.2:p.Phe166Tyr
|
|
ENST00000335475.6:c.116T>A
|
ENSP00000334497.5:p.Phe39Tyr
|
|
ENST00000646564.1:c.124-12788T>A
|
ENSP00000495806.1:n.124-12788T>A
|
|
ENST00000155840.9:c.497T>A
|
ENSP00000155840.2:p.Phe166Tyr
|
|
ENST00000335475.5:c.116T>A
|
ENSP00000334497.5:p.Phe39Tyr
|
|
ENST00000496887.6:c.236T>A
|
ENSP00000434560.1:p.Phe79Tyr
|
|
NM_000218.2:c.497T>A , LRG_287t1:c.497T>A
|
NP_000209.2:p.Phe166Tyr
|
|
NM_181798.1:c.116T>A , LRG_287t2:c.116T>A
|
NP_861463.1:p.Phe39Tyr
|
|
NM_000218.3:c.497T>A
MANE Select
|
NP_000209.2:p.Phe166Tyr
|
|